Skip to content

About the Authors


Renée A. Beach, MD, FRCPC

Dr. Beach is an adjunct Assistant Professor in the University of Toronto’s Faculty of Medicine. She completed her medical training at McMaster University (MD) and dermatology residency at the University of Ottawa. She practices medical and cosmetic dermatology at her recently opened practice DermAtelier on Avenue in Toronto. At Women’s College Hospital, she teaches dermatology residents in the Consultative Hair Loss Clinic.


Kikachukwu Otiono, B.A. MD Candidate, Michael G. DeGroote School of Medicine, McMaster University (Class of 2022)

Ms. Otiono is a 2nd year medical student at the Michael G. DeGroote School of Medicine at McMaster University. She is a native of Ottawa and the Director of Advocacy & Representation for the Black Medical Students’ Association of Canada (BMSAC).

Canadian Dermatology Today, Volume 1, Issue 4, November 2020

A Tale of Two Frontal Alopecias: Traction Alopecia and Frontal Fibrosing Alopecia – Clinical Pearls and Promising Therapies


Traction alopecia (TA) is a form of hair loss caused by repetitive tension and pulling of the hair.1 TA most commonly occurs in women of Afro-Caribbean descent with afro-textured hair due to the higher prevalence of high-tension hairstyles such as braids and weaves.2 However, it has also been reported in other patient demographics including ballerinas3, gymnasts, and patients with certain head coverings.4 TA typically occurs in a biphasic nature, starting with an early stage that is non-cicatricial (without scarring) which can progress to cicatricial and permanent alopecia with prolonged tension.5 Conversely, frontal fibrosing alopecia (FFA) is a variant of lichen planopilaris (LPP) that presents as an inflammatory cicatricial alopecia. FFA is clinically characterized by permanent alopecia, an unpredictable clinical course, and a band-like pattern of involvement in the frontal and temporal hairline.6 FFA mainly affects post-menopausal women as described by Kossard,7  although there have been cases reported in premenopausal women and in men.8 

When hair loss involves the frontotemporal region, it can sometimes be difficult to distinguish between TA and FFA. Marginal or frontal hairline TA can especially mimic the band-like pattern of hair loss seen in FFA. As such, delineation of the clinical presentations and distinguishing features of each condition is important.  This paper outlines clinical parameters for each diagnosis to enable accurate diagnosis and therapy. 

Clinical Examination 

Traction alopecia (TA) is directly related to mechanical trauma and repetitive pulling from high-tension hairstyles, therefore it is crucial to elicit haircare practices during history-taking.  Women with afro-textured hair are at highest risk due to the increased prevalence of high-risk hairstyles such as twists, braids, cornrows, weaves which are installed with tension and involve added hair, and dreadlocks which can be heavy as they mature and lengthen.9,10 Chemical relaxation/hair straightening products coupled with artificial extensions are also strongly associated with increased risk of TA.10 This increased risk occurs because the existing hair is permanently weakened, and tension-based styles or added hair further strain the hair strands. It is important to note that although TA is more prevalent in Afro-Caribbean patients, this is more related to common haircare practices rather than afro-textured hair types, as similar haircare practices yield symptomatology in other groups. Examples include tight buns and ponytails, religious practices (e.g. hair twisting in Sikh boys and men), tight scarf styles, extensions,11 curlers, and chignon.3

The clinical features of traction alopecia depend heavily on the level of mechanical trauma and the stage of the disease. The most common presentation of TA is marginal alopecia which affects the frontal and temporal scalp, while the less common nonmarginal alopecia results in hair loss in other areas like the interior scalp.1 In the earliest stages, patients will admit to sustaining pain or a headache after hairstyle installation. TA is non-scarring and may present as a slight decrease in hair density or small alopecic patches. Among the earliest clinical signs is the presence of traction folliculitis, producing perifollicular erythema, papules, and pustules in areas with the highest tension.12 The ‘fringe sign’ is typically present, which is characterized by fine or miniaturized hairs remaining at the margin of the frontal hairline with hair loss posterior to the fringe.13   There may also be hair casts, which are thin, white-hued cylindrical concretions that surround the hair shaft.14 Permanent alopecia may occur with persistent mechanical trauma.

Unlike the mechanical pathogenesis of TA, frontal fibrosing alopecia (FFA) is a primary cicatricial alopecia. The pathogenesis of FFA is poorly understood, but LPP in general is believed to occur via an inflammatory process.15 Overall, LPP seems to be more common in women than in men.16 The classic presentation of FFA is a band-like hair loss in the frontotemporal hairline in post-menopausal women.17-19 FFA can also affect premenopausal women, and rarely, men.6 Multiple studies have also demonstrated a strong association between thyroid disease (especially hypothyroidism) and FFA.21,22

Although, the band-like distribution of FFA predominantly occurs in the frontal hairline, scarring can extend to the preauricular and retro-auricular regions of the scalp.23 It can also affect other areas including the occipital region and the auricular margins.24 While TA affects only the area of the scalp under tension, FFA commonly causes hair loss in eyebrows as well. In male patients affected by FFA, there may be hair loss in the frontal hairline, eyebrows, beard area and sideburns.25 Clinicians may also notice a small number of isolated or solitary hairs within the band of alopecia, often referred to as the ‘lonely hair sign.’26 Other clinical features include erythematous and hyperkeratotic follicular openings, hypopigmentation,27 and trichodynia28 in patients with white skin.  Interestingly, patients with brown skin and afro-textured hair generally display less erythema and may show perifollicular hyperpigmentation instead.


Since TA has a biphasic course, histopathological findings differ based on the severity and stage of alopecia.  Early TA is characterized by a normal number of vellus hairs, trichomalacia, and a decrease in telogen and catagen follicles.29   Late-stage TA results in scarring with reduced follicular density, retained sebaceous glands, and a decrease in terminal follicle count (follicular ‘drop out’).29  Conversely, primary cicatricial alopecias such as FFA feature the replacement of destroyed follicular units with fibrous tissues30 as well as loss of follicular ostia.31 FFA is a lymphocytic primary cicatricial alopecia with perifollicular inflammation and lymphocytic cell infiltrate at the infundibulum and isthmus.32 

Therapeutic Management

Both types of alopecia can be managed according to their clinical severity and progression, as well as patient preference for non-prescription versus prescription-based management (Table 1).

Table 1: Management of traction alopecia (TA) and frontal fibrosing alopecia (FFA) *Off-label therapy

Behavioural Management

For both forms of alopecia, minimizing damage to the frontal scalp is critical.  In TA, minimization, if not avoidance, of hair styles with tension or pulling is paramount. Varying scalp parts for typical hairstyles or wearing the hair in a looser style, such as a low bun is helpful.33 For women and men who wear headgear for religious observance, adjustments like applying a cotton band to the hairline, then the turban or hijab afterwards will help relieve tension.  In FFA, there is some association of its provocation following mechanical or thermal trauma to the scalp.34 Australian dermatologists have proposed an association between FFA and the application of sunscreen to the hairline, including hair regrowth following its stoppage.35 Therefore, avoidance of these potential triggers at these scalp sites is preferred.  

Topical therapy

In TA and FFA, topical therapy can be used to limit inflammation, particularly in the early stages of the condition, or if there are symptoms of erythema, tenderness, and edema. Use of medium potency steroids like betamethasone valerate 0.1% lotion can help abate clinical symptoms in TA and FFA. Removal of the inciting hairstyle and use of topical minoxidil preparations can stimulate hair regrowth in TA.36

Procedural therapy

Reports of hair regrowth following injection of triamcinolone acetonide 5 mg/mL (Kenalog) to the affected scalp in TA make it a feasible in-office therapy at 6-8-week intervals.37 However, patients risk pain and injection site atrophy. Also, it must be emphasized that this is not curative or a substitution for adaptation of tension-free hairstyling. In FFA, the use of Kenalog therapy at 8–12 week intervals is considered a cornerstone of management. It is postulated to help negate the presence and activity of inflammatory cytokines.38   There are limited reports of platelet rich plasma (PRP) showing success in FFA for cessation of symptoms and hair regrowth.39   Patients should be informed of its out-of-pocket cost and potential to require ongoing maintenance sessions to maintain its effect. 

Oral Therapy

Although not the cornerstone of therapy, there is evidence that off-label use of oral minoxidil 1.25 – 2.5 mg at night can result in hair regrowth in non-scarred TA patients.40 Results are noted after 3-6 months of consistent use.  Patients should be advised of the risk of extra-scalp hypertrichosis. There are a range of oral therapies for FFA, many of which are similar to LPP. In the acute phase, short courses of tetracycline antibiotic doxycycline may be helpful in diminishing scalp erythema and inflammatory symptoms. Successful treatment of LPP with immunomodulators such as cyclosporine, methotrexate, and mycophenolate mofetil has been reported and each yield better clinical improvement than hydroxychloroquine.41 Given its relation to lichen planus, therapy with the retinoid acitretin can be a therapeutic option which also avoids immunosuppression.  However, patients should be educated about the potential for telogen effluvium with this treatment.  Finasteride treatment can be helpful, perhaps due to concurrent androgenetic alopecia activity.  Finally, use of immune-modifiers like pioglitazone have a therapeutic role, particularly for patients who have clinical symptoms associated with their hair loss.42

Surgical Treatment

There are successful reports of TA correction with hair transplant in patients with afro-textured hair and straight hair.43,44 While FFA, if stable for 12 months, can undergo hair transplant,  scalp surgery has also been associated with inciting FFA,45 and thus must be considered as a last resort therapy with a patient who fully understands the potential for a paradoxical result. 


These two forms of hair loss, TA and FFA, share a predilection for the frontal scalp and overlapping therapeutic options.  Dermatologists’ clinical acumen and therapeutic experience are best suited to confirm their diagnoses and optimize therapy.  The descriptions of their clinical findings, histological features, and management options provided here are a framework to help provide comprehensive clinical management and improvement. 


1. Billero V, Miteva M. Traction alopecia: the root of the problem. Clinical, Cosmetic and Investigational Dermatology. 2018;Volume 11:149-159. doi:10.2147/ccid.s137296

2. Wright DR, Gathers R, Kapke A, Johnson D, Joseph CL. Hair care practices and their association with scalp and hair disorders in African American girls. Journal of the American Academy of Dermatology. 2011;64(2):253-262. doi:10.1016/j.jaad.2010.05.037

3. Samrao A, Chen C, Zedek D, Price VH. Traction alopecia in a ballerina: clinicopathologic features. Arch Dermatol. 2010;146(8):930-931. doi:10.1001/archdermatol.2010.183

4. Hwang SM, Lee WS, Choi EH, Lee SH, Ahn SK. Nurse’s cap alopecia. Int J Dermatol. 1999;38(3):187-191. doi:10.1046/j.1365-4362.1999.00556.x

5. Mirmirani P, Khumalo N-P. Traction alopecia: how to translate study data for public education–closing the KAP gap?. Dermatologic clinics. 2014; 32(2) :153-161.

6. Rongioletti F, Christana K. Cicatricial (Scarring) Alopecias. American Journal of Clinical Dermatology. 2012;13(4):247-260. doi:10.2165/11596960-000000000-00000

7. Kossard S, Lee M-S, Wilkinson B. Postmenopausal frontal fibrosing alopecia: A frontal variant of lichen planopilaris. Journal of the American Academy of Dermatology. 1997;36(1):59-66. doi:10.1016/s0190-9622(97)70326-8

8. Algaadi S, Miteva M, Tosti A. Frontal fibrosing alopecia in a male presenting with sideburn loss. International Journal of Trichology. 2015;7(2):72. doi:10.4103/0974-7753.160115

9. Ahdout J, Mirmirani P. Weft hair extensions causing a distinctive horseshoe pattern of traction alopecia. Journal of the American Academy of Dermatology. 2012;67(6). doi:10.1016/j.jaad.2012.07.020

10. Khumalo NP, Jessop S, Gumedze F, Ehrlich R. Determinants of marginal traction alopecia in African girls and women. Journal of the American Academy of Dermatology. 2008;59(3):432-438. doi:10.1016/j.jaad.2008.05.036

11. Yang A, Iorizzo M, Vincenzi C, Tosti A. Hair extensions: a concerning cause of hair disorders. British Journal of Dermatology. 2009;160(1):207-209. doi:10.1111/j.1365-2133.2008.08924.x

12. Fox GN, Stausmire JM, Mehregan, DR. Traction folliculitis: an underreported entity. Cutis. 2007; 79(1), 26-30. (2007). Traction folliculitis: an underreported entity. Cutis, 79(1), 26–30.

13. Samrao A, Price VH, Zedek D, Mirmirani P. The “Fringe Sign” – A useful clinical finding in traction alopecia of the marginal hair line. Dermatol Online J. 2011;17(11):1. Published 2011 Nov 15.

14. Tosti A, Miteva M, Torres F, Vincenzi C, Romanelli P. Hair casts are a dermoscopic clue for the diagnosis of traction alopecia. Br J Dermatol. 2010;163(6):1353-1355. doi:10.1111/j.1365-2133.2010.09979.x

15. Mobini N, Tam S, Kamino H. Possible role of the bulge region in the pathogenesis of inflammatory scarring alopecia: lichen planopilaris as the prototype. J Cutan Pathol. 2005;32(10):675-679. doi:10.1111/j.0303-6987.2005.00399.x

16. Mehregan DA, Van Hale HM, Muller SA. Lichen planopilaris: clinical and pathologic study of forty-five patients. J Am Acad Dermatol. 1992;27(6 Pt 1):935-942. doi:10.1016/0190-9622(92)70290-v

17. Vañó-Galván S, Molina-Ruiz AM, Serrano-Falcón C, et al. Frontal fibrosing alopecia: a multicenter review of 355 patients. J Am Acad Dermatol. 2014;70(4):670-678. doi:10.1016/j.jaad.2013.12.003

18. MacDonald A, Clark C, Holmes S. Frontal fibrosing alopecia: a review of 60 cases. J Am Acad Dermatol. 2012;67(5):955-961. doi:10.1016/j.jaad.2011.12.038

19. Tosti A, Piraccini BM, Iorizzo M, Misciali C. Frontal fibrosing alopecia in postmenopausal women. J Am Acad Dermatol. 2005;52(1):55-60. doi:10.1016/j.jaad.2004.05.014

20. Elloudi S, Meziane M, Mernissi F. Alopécie frontale fibrosante : étude prospective de 20 cas [Frontal fibrosing alopecia: A prospective study of 20 cases]. Annales de Dermatologie et de Vénéréologie. 2015;142(12). doi:10.1016/j.annder.2015.10.321

21. Valesky EM, Maier MD, Kaufmann R, Zöller N, Meissner M. Single-center analysis of patients with frontal fibrosing alopecia: evidence for hypothyroidism and a good quality of life. J Int Med Res. 2019;47(2):653-661. doi:10.1177/0300060518807335

22. Nguyen TQ, Tsai M, Goh C. Thyroid disease in alopecia areata, lichen planopilaris, and frontal fibrosing alopecia – a case control of 144 patients. US Endocrinology, 2016; 12(2), 85-86.

23. Litaiem N, Idoudi S. Frontal Fibrosing Alopecia. National Centre for Biotechnology Information (NCBI). Updated Aug 10, 2020. Accessed September 2, 2020. 

24. Callender VD, Reid SD, Obayan O, Mcclellan L, Sperling L. Diagnostic Clues to Frontal Fibrosing Alopecia in Patients of African Descent. J Clin Aesthet Dermatol. 2016;9(4):45-51.

25. Stockmeier M, Kunte C, Sander CA, Wolff H. Frontale fibrosierende Alopezie Kossard bei einem Mann [Kossard frontal fibrosing alopecia in a man]. Hautarzt. 2002;53(6):409-411. doi:10.1007/s001050100273

26. Tosti A, Miteva M, Torres F. Lonely hair: a clue to the diagnosis of frontal fibrosing alopecia. Arch Dermatol. 2011;147(10):1240. doi:10.1001/archdermatol.2011.261

27. Lin J, Valdebran M, Bergfeld W, Conic RZ, Piliang M, Atanaskova Mesinkovska N. Hypopigmentation in frontal fibrosing alopecia. J Am Acad Dermatol. 2017;76(6):1184-1186. doi:10.1016/j.jaad.2017.01.001

28. Vañó-Galván S, Molina-Ruiz AM, Serrano-Falcón C, et al. Frontal fibrosing alopecia: a multicenter review of 355 patients. J Am Acad Dermatol. 2014;70(4):670-678. doi:10.1016/j.jaad.2013.12.003

29. Ngwanya RM, Adeola HA, Beach RA, et al. Reliability of Histopathology for the Early Recognition of Fibrosis in Traction Alopecia: Correlation with Clinical Severity. Dermatopathology (Basel). 2019;6(2):170-181. Published 2019 Jun 26. doi:10.1159/000500509

30. Stefanato CM. Histopathology of alopecia: a clinicopathological approach to diagnosis. Histopathology. 2010;56(1):24-38. doi:10.1111/j.1365-2559.2009.03439.x

31. Tan E, Martinka M, Ball N, Shapiro J. Primary cicatricial alopecias: clinicopathology of 112 cases. J Am Acad Dermatol. 2004;50(1):25-32. doi:10.1016/j.jaad.2003.04.001

32. Sperling LC, Cowper SE. The Histopathology of Primary Cicatricial Alopecia. Seminars in Cutaneous Medicine and Surgery. 2006;25(1):41-50. doi:10.1016/j.sder.2006.01.006

33. Haskin A, Aguh C. All hairstyles are not created equal: What the dermatologist needs to know about black hairstyling practices and the risk of traction alopecia (TA). J Am Acad Dermatol. 2016;75(3):606-611. doi:10.1016/j.jaad.2016.02.1162

34. Chiang YZ, Tosti A, Chaudhry IH, et al. Lichen planopilaris following hair transplantation and face-lift surgery. Br J Dermatol. 2012;166(3):666-370. doi:10.1111/j.1365-2133.2011.10692.x

35. Cranwell WC, Sinclair R. Frontal fibrosing alopecia: Regrowth following cessation of sunscreen on the forehead. Australas J Dermatol. 2019;60(1):60-61. doi:10.1111/ajd.12833

36. Stoehr JR, Choi JN, Colavincenzo M, Vanderweil S. Off-Label Use of Topical Minoxidil in Alopecia: A Review. Am J Clin Dermatol. 2019;20(2):237-250. doi:10.1007/s40257-018-0409-y

37. Uwakwe LN, De Souza B, Tovar-Garza A, McMichael AJ. Intralesional Triamcinolone Acetonide in the Treatment of Traction Alopecia. J Drugs Dermatol. 2020;19(2):128-130. doi:10.36849/JDD.2020.4635

38. Gkini MA, Riaz R, Jolliffe V. A Retrospective Analysis of Efficacy and Safety of Intralesional Triamcinolone Injections in the Treatment of Frontal Fibrosing Alopecia Either as Monotherapy or as a Concomitant Therapy. Int J Trichology. 2018;10(4):162-168. doi:10.4103/ijt.ijt_46_18

39. Özcan D, Tunçer Vural A, Özen Ö. Platelet-rich plasma for treatment resistant frontal fibrosing alopecia: A case report. Dermatol Ther. 2019;32(5):e13072. doi:10.1111/dth.13072

40. Beach RA. Case series of oral minoxidil for androgenetic and traction alopecia: Tolerability & the five C’s of oral therapy. Dermatol Ther. 2018;31(6):e12707. doi:10.1111/dth.12707

41. Babahosseini H, Tavakolpour S, Mahmoudi H, et al. Lichen planopilaris: retrospective study on the characteristics and treatment of 291 patients. J Dermatolog Treat. 2019;30(6):598-604. doi:10.1080/09546634.2018.1542480

42. Baibergenova A, Walsh S. Use of pioglitazone in patients with lichen planopilaris. J Cutan Med Surg. 2012;16(2):97-100. doi:10.2310/7750.2011.11008

43. Okereke UR, Simmons A, Callender VD. Current and emerging treatment strategies for hair loss in women of color. Int J Womens Dermatol. 2019;5(1):37-45. Published 2019 Jan 23. doi:10.1016/j.ijwd.2018.10.021

44. Ozçelik D. Extensive traction alopecia attributable to ponytail hairstyle and its treatment with hair transplantation. Aesthetic Plast Surg. 2005;29(4):325-327. doi:10.1007/s00266-005-0004-5

45. Chiang YZ, Tosti A, Chaudhry IH, et al. Lichen planopilaris following hair transplantation and face-lift surgery. Br J Dermatol. 2012;166(3):666-370. doi:10.1111/j.1365-2133.2011.10692.x